Université Paris Diderot
12 imported, source-linked research records. All imported publication dates.
12 matching research records
Topic: Mitochondrial DNA mutations. Only records linked to Université Paris Diderot are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–12 of 12 matching records. Counts update as records arrive.
Darwinian selection within an individual or somatic selection: facts and models
February 18, 2019 · 4 citations · Open access
Open original record →Further quantitative insights into the decrease of heteroplasmy of m.3243A G with age in leukocytes
January 28, 2019 · 4 citations
Open original record →Diagnosis of ‘possible’ mitochondrial disease: an existential crisis
January 25, 2019 · 66 citations · Open access
Open original record →Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls
October 17, 2018 · 39 citations · Open access
Open original record →How the most common mitochondrial DNA mutation (m.3243A G) vanishes from leukocytes: a mathematical model
February 19, 2018 · 7 citations · Open access
Open original record →Diversity of Pneumocystis jirovecii during Infection Revealed by Ultra-Deep Pyrosequencing
May 24, 2016 · 50 citations · Open access
Open original record →Aging of the dopaminergic system and motor behavior in mice intoxicated with the parkinsonian toxin 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine
June 18, 2012 · 12 citations · Open access
Open original record →Impact and Mechanisms of Pancreatic Beta-Cell Mass Programming by Maternal Diabetes - Insight from Animal Model Studies
November 2, 2011 · 4 citations · Open access
Open original record →Early-Life Origins of Type 2 Diabetes: Fetal Programming of the Beta-Cell Mass
January 1, 2011 · 127 citations · Open access
Open original record →The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes
May 27, 2009 · 96 citations
Open original record →Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study
June 25, 2008 · 46 citations · Open access
Open original record →Role of mitochondria in non‐alcoholic fatty liver disease
May 29, 2007 · 279 citations
Open original record →